Skip to main content
PMC home page
PLOS ONE logoLink to PLOS ONE
. 2015 Mar 27;10(3):e0120261. doi: 10.1371/journal.pone.0120261

Human Dendritic Cell DC-SIGN and TLR-2 Mediate Complementary Immune Regulatory Activities in Response to Lactobacillus rhamnosus JB-1

Patrycja Konieczna 1, Elisa Schiavi 1, Mario Ziegler 1, David Groeger 2, Selena Healy 2, Ray Grant 3, Liam O’Mahony 1,*
Editor: Hossam M Ashour4
PMCID: PMC4376398  PMID: 25816321

Abstract

The microbiota is required for optimal host development and ongoing immune homeostasis. Lactobacilli are common inhabitants of the mammalian large intestine and immunoregulatory effects have been described for certain, but not all, strains. The mechanisms underpinning these protective effects are beginning to be elucidated. One such protective organism is Lactobacillus rhamnosus JB-1 (Lb. rhamnosus JB-1). Lb. murinus has no such anti-inflammatory protective effects and was used as a comparator organism. Human monocyte-derived dendritic cells (MDDCs) were co-incubated with bacteria and analysed over time for bacterial adhesion and intracellular processing, costimulatory molecule expression, cytokine secretion and induction of lymphocyte polarization. Neutralising antibodies were utilized to identify the responsible MDDC receptors. Lb. rhamnosus JB-1 adhered to MDDCs, but internalization and intracellular processing was significantly delayed, compared to Lb. murinus which was rapidly internalized and processed. Lb. murinus induced CD80 and CD86 expression, accompanied by high levels of cytokine secretion, while Lb. rhamnosus JB-1 was a poor inducer of costimulatory molecule expression and cytokine secretion. Lb. rhamnosus JB-1 primed MDDCs induced Foxp3 expression in autologous lymphocytes, while Lb. murinus primed MDDCs induced Foxp3, T-bet and Ror-γt expression. DC-SIGN was required for Lb. rhamnosus JB-1 adhesion and influenced IL-12 secretion, while TLR-2 influenced IL-10 and IL-12 secretion. Here we demonstrate that the delayed kinetics of bacterial processing by MDDCs correlates with MDDC activation and stimulation of lymphocytes. Thus, inhibition or delay of intracellular processing may be a novel strategy by which certain commensals may avoid the induction of proinflammatory responses.

Introduction

It is well accepted that the gut microbiota plays a pivotal role in mucosal immune system development and ongoing homeostasis [1–3]. Moreover, a diverse gut microbiota contributes to appropriate digestion of dietary substances, protects against pathobiont expansion, provides nutrients for the host and ensures appropriate development of the mucosal barrier [4–6]. The mechanisms underpinning these protective responses are varied and include not only intact microbial cell interaction with host receptors, but also microbial metabolic activity, including short chain fatty acid production and bile degradation, which influences biological functions of the whole organism [7–9].

Crosstalk between the microbiota and the host is tightly regulated. Expression of pattern recognition receptors (PRRs) allows the immune system to discriminate between commensal and harmful microbes. Activation of diverse PRRs leads to differential cascades in signaling pathways and subsequently polarized secretion of cytokines and metabolites. Certain protective microbes interact with mucosal cells and contribute to the maintenance of mucosal tolerance [10–12]. In recent years, Lactobacilli strains have been repeatedly shown to have many beneficial effects within the gut [13]. Many diverse species and strains have been well characterized. Lactobacillus rhamnosus JB-1 (Lb. rhamnosus JB-1) has been well described as a tolerogenic commensal microbe, with multiple effects on mucosal cells including the induction of Foxp3+ T regulatory cells [14–16]. In addition, this microbe exerts potent effects on the gut-brain axis [17]. However, not all Lactobacillus strains exert the same effects, for example Lactobacillus salivarius AH102 does not induce T regulatory cells [18].

The molecular mechanisms underpinning the tolerogenic effects of Lactobacilli are diverse and are only beginning to be described in detail. Peptidoglycan-associated muropeptide produced by Lactobacillus salivarius Ls33 is thought to be responsible for its anti-inflammatory effect [19]. Lipoteichoic acid D-alanylation decreases anti-inflammatory responses associated with Lactobacillus plantarum and Lactobacillus acidophilus [20, 21]. Following removal of this modification, mutants were more efficient in their ability to protect against colitis in murine models. Moreover, secreted proteins such as p40 and p70 from Lactobacillus rhamnosus GG have been shown to enhance a functional epithelial barrier and improve cell survival [22–24]. Even small differences, such as glycosylation patterns, in cell-wall composition can lead to opposing effects on immune responsiveness [25, 26]. Indeed, the amount of a specific metabolite being secreted by a specific strain can have protective or pathological effects on the host immune system. For example, a Lb. rhamnosus strain, which secretes a low level of histamine, exerts protective immunological effects, while a Lb. saerimneri strain, which secretes high levels of histamine, induces an inflammatory response within the gut [27, 28]. However it is likely that many more, yet undiscovered, molecular mechanisms are involved and the data so far suggest that many of these mechanisms are bacterial strain and context dependent.

This diversity in molecular mechanisms is important, not least because mucosal recognition of bacterial strains via multiple PRRs on dendritic cells (DCs) will lead to divergent and polarized adaptive responses [29]. Typically, DCs will bind bacteria, internalize the microbe, lyse the bacterium within activated lysosomes and present the microbial antigens in the context of MHC. This response is accompanied by upregulation of costimulatory molecules and cytokine secretion in order to induce the appropriate tissue and adaptive immune responses. However, the combined examination of DC processing and cytokine secretion, in response to Lactobacilli strains, has not been previously described. In this report, we demonstrate an association between delayed DC intracellular processing of Lb. rhamnosus JB-1, which is associated with poor induction of costimulatory molecule expression and cytokine secretion, with preferential induction of Foxp3+ lymphocytes and no induction of TH1 or TH17 transcription factors. These responses are partially mediated via TLR-2 and DC-SIGN.

Results

MDDCs efficiently bind Lb. rhamnosus JB-1, but display delayed internalization and processing

Human monocyte-derived dendritic cells (MDDCs) efficiently bind Lb. rhamnosus JB-1 as demonstrated by multispectral image stream analysis (Fig. 1A). In order to examine Lb. rhamnosus JB-1 internalisation and processing in more detail, we further examined MDDC responses to this microbe over an extended timeframe using confocal microscopy (Fig. 1B). Surprisingly, MDDCs did not internalize Lb. rhamnosus JB-1 for at least 48 hours following co-incubation, despite binding a large number of microbes on the cell surface. In addition, the binding pattern was unusual as distinct clustering of the bound microbe around the nucleus of the MDDCs was evident, even up to 96 hours following co-incubation. This delay in processing of Lb. rhamnosus JB-1 was not oberserved for an unrelated Lb. murinus strain (Fig. 1C), while the peri-nuclear binding was also not observed for Lb. murinus. Internalization of Lb. rhamnosus JB-1 was shown to peak at 48 hours as antibiotic treatment of the dendritic cells kills bacteria on the surface of the cells, while internalized bacteria are protected from the antibiotic allowing their growth and enumeration on agar plates (Fig. 2A). In addition, phagocytosis of fluorescently labeled E. coli was delayed in Lb. rhamnosus JB-1 treated dendritic cells, but not in Lb. murinus treated dendritic cells (Fig. 2B).

Fig 1. Differential MDDC binding and processing of two Lactobacilli strains.

Fig 1

Open in a new tab

MDDCs bind Lb. rhamnosus JB-1 efficiently but intracellular processing is delayed, as visualized by multispectral flow cytometry imaging (A) and confocal microscopy (B). Lb. murinus is also efficiently bound by MDDCs and is rapidly processed (C). For both strains, bacterial cells are CFSE labeled (green), while CD11c+ cells are PE-Cy5 stained (red).

Fig 2. Lb. rhamnosus JB-1 internalisation by MDDCs.

Fig 2

Open in a new tab

(A) Following antibiotic treatment, which kills bacteria outside MDDCs, the peak recovery of viable Lb. rhamnosus JB-1 was observed after 48 hours, suggesting that this was the time point when the bacteria were internalized by the MDDCs. (B) MDDC phagocytosis of another bacterial strain, E. coli, was reduced when the MDDCs were co-exposed to Lb. rhamnosus JB-1, but not Lb. murinus.

Distinct MDDC responses are induced by two Lactobacillus strains

Following activation, MDDCs upregulate expression of cell surface co-stimulatory molecules and secrete cytokines. LPS stimulation resulted in robust stimulation of CD80/CD86 double positive MDDCs, followed by Lb. murinus, while Lb. rhamnosus JB-1 was a poor inducer of CD80/CD86 expression (Fig. 3A). Lb. rhamnosus JB-1-stimulated expression of CD80 and CD86 was significantly less than that induced by LPS or Lb. murinus.

Fig 3. MDDC costimulatory molecule expression and cytokine secretion.

Fig 3

Open in a new tab

(A) CD80 and CD86 were upregulated on MDDCs after exposure to both bacterial strains. LPS served as a positive control. Co-stimulatory molecule expression was significantly higher after stimulation with Lb. murinus compared with Lb. rhamnosus JB-1. (B) Lb. murinus stimulated MDDC cytokine secretion was significantly higher, for all cytokines tested, compared to that induced by Lb. rhamnosus JB-1 (n = 5 donors). *p<0.05

MDDCs were co-incubated with 1x105 or 1x106 bacterial cells, and their supernatant cytokine levels were quantified after 24 hours. Lb. murinus induced high levels of TNF-α, IL-6, IL-10, IL-12p70, G-CSF and MCP-1. However, stimulation with Lb. rhamnosus JB-1 resulted in significantly less cytokine secretion, for all the cytokines measured (Fig. 3B). The relatively poor induction of co-stimulatory molecule expression and cytokine secretion by Lb. rhamnosus JB-1 is consistent with the imaging results, whereby the dendritic cell response to this bacterium seems to be minimal. SOCS3 has been previously described to suppress cytokine responses via negative regulation of MAP kinase activation. Lb. rhamnosus JB-1-stimulated MDDCs upregulated SOCS gene expression and p38 MAPK responses were significantly less than for LPS stimulated cells (S1 Fig.).

In order to further compare and contrast the dendritic cell response to these two lactobacilli strains, we co-incubated bacterial-stimulated dendritic cells with autologous lymphocytes for 7 days. Both Lb. rhamnosus JB-1 and Lb. murinus-stimulated MDDCs induced Foxp3 expression in autologous lymphocyte (Fig. 4). However, Lb. murinus-stimulated MDDCs also induced expression of T-bet (TH1) and ror-γt (TH17) transcription factors (Fig. 4). Lb. rhamnosus JB-1-stimulated MDDCs did not alter expression of the TH1 or TH17 transcription factors in autologous lymphocytes, when compared to transcription factor levels in control cultures (i.e. non-stimulated MDDCs and autologous lymphocytes co-incubation for 7 days).

Fig 4. Transcription factor expression in lymphocytes co-incubated with bacterial primed MDDCs.

Fig 4

Open in a new tab

Following 7 days co-incubation, MDDCs primed by both bacterial strains induced CD25+Foxp3+ T regulatory cells, while only MDDCs exposed to Lb. murinus increased T-bet and Ror-γt positive CD4+ T cells.

DC-SIGN, but not TLR-2, is required for Lb. rhamnosus JB-1 binding to MDDCs

In order to further investigate the receptors that may be involved in MDDC recognition of Lb. rhamnosus JB-1, we specifically examined the role for DC-SIGN and TLR-2 as they have been previously shown by us and others to recognize commensal and pathogenic microbes. Firstly we assessed if c-type lectin receptors (CLRs) are required by comparing MDDC binding under calcium free conditions. MDDC capture of Lb. rhamnosus JB-1 was reduced by approximately 55% when calcium was absent from the medium suggesting that CLRs might be involved (Fig. 5A). DC-SIGN is a CLR previously described to recognize certain lactobacillus strains. When DC-SIGN was blocked using a neutralizing antibody, Lb. rhamnosus JB-1 adhesion to MDDCs was significantly reduced and the peri-nuclear clustering pattern was substantially reduced (Fig. 5B). However, neutralization of TLR-2 had no effect on Lb. rhamnosus JB-1 adhesion (Fig. 5B).

Fig 5. Lb. rhamnosus JB-1 is bound by MDDC DC-SIGN.

Fig 5

Open in a new tab

(A) Lb. rhamnosus JB-1 binding to MDDCs is partially dependent on the presence of Ca2+ ions, suggesting the involvement of CLRs. The flow cytometry plots are representative of 3 independent experiments. (B) As visualized by confocal microscopy, blockade of DC-SIGN decreased Lb. rhamnosus JB-1 binding to MDDC, while neutralizing TLR-2 antibodies had no effect on Lb. rhamnosus JB-1 binding.

Lb. rhamnosus JB-1 stimulation of MDDC cytokine secretion is DC-SIGN and TLR-2 dependent

MDDCs were pre-incubated with specific blocking antibodies for TLR-2 or DC-SIGN prior to bacteria stimulation and cytokine secretion was analyzed after 24 hours. Inhibition of TLR-2 signalling resulted in significantly decreased secretion of IL-10, associated with increased secretion of IL-12p70 in response to Lb. rhamnosus JB-1 (Fig. 6A). However, neutralization of TLR-2 activation did not alter the IL-10 or IL-12 response to Lb. murinus (Fig. 6A). Blockade of DC-SIGN had no effect on IL-10 or TNF-α secretion, while IL-12p70 secretion in response to Lb. rhamnosus JB-1 was significantly reduced. DC-SIGN neutralization had no effect on Lb. murinus-stimulated MDDC cytokine responses (Fig. 6A). We further confirmed that TLR-2 recognises Lb. rhamnosus JB-1 by utilizing HEK-293 cells, which express TLR-2. These cells responded to Lb. rhamnosus JB-1, as demonstrated by an increase in NF-κB/AP-1 activation, while neutralizing TLR-2 antibodies significantly reduced this response (Fig. 6B). In addition, TLR-2 deficient HEK-293 did not respond to Lb. rhamnosus JB-1 (Fig. 6B). MDDCs also express high levels of Dectin-1 and we performed blocking experiments for this receptor to investigate its role in cytokine secretion in response to Lb. rhamnosus JB-1. However, there was no significant difference in cytokine production following Dectin-1 neutralisation (data not shown).

Fig 6. MDDC TLR-2 and DC-SIGN are required for appropriate cytokine responses to Lb. rhamnosus JB-1.

Fig 6

Open in a new tab

(A) Lb. rhamnosus JB-1 or Lb. murinus-stimulated MDDCs were pre-incubated with blocking antibodies for TLR-2 (n = 8 donors), DC-SIGN (n = 8 donors) or antibody isotype controls for 30 minutes prior to stimulation and cytokine secretion was analyzed after 24 hours. Results are expressed as the mean pg/ml +/− standard error. (B) TLR-2 activation was confirmed using HEK-293 cells which express TLR-2. *p<0.05

Discussion

In this report we demonstrate that the kinetics of DC processing and the magnitude of cellular activation induced by Lb. rhamnosus JB-1 are significantly different than that of another strain, Lb. murinus. At least two different PRRs are involved in this response, DC-SIGN and TLR-2. Even though Lb. rhamnosus JB-1 does not strongly stimulate DC responses, primed DCs are capable of inducing Foxp3 expression in lymphocytes. Lb. murinus primed DCs also induce Foxp3 expression but this is associated with T-bet and ror-γt expression.

These data suggest that one mechanism that may be exploited by Lb. rhamnosus JB-1 to prevent excessive inflammatory responses against this non-pathogenic microbe is to suppress DC activation. The data also suggest that this is an active process, rather than a passive process whereby the strain is simply not recognized by the DC. Blockade of TLR-2 results in less IL-10 being secreted, but more IL-12p70, a TH1 associated cytokine. In contrast, blockade of DC-SIGN results in reduced secretion of IL-12p70. This suggests that TLR-2 and DC-SIGN activation both influence different aspects of the DC response to Lb. rhamnosus JB-1.

TLR-2 is widely described as a PRR mediating host protective immune responses. In general, TLR-2−/− DCs are not efficient in promoting Foxp3 Treg cell development and IL-10 secretion in vitro [30, 31]. Moreover, TLR-2-/- mice are more susceptible to DSS- induced colitis. TLR-2 activation by Lb. rhamnosus JB-1 is required for IL-10 secretion, while TLR-2 activation suppresses IL-12p70. The link between TLR-2 activation and suppression of IL-12 or CXCL-10 is unknown, however, SOCS3 gene expression is increased by Lb. rhamnosus JB-1-stimulated MDDCs. SOCS3 has been previously described to suppresses p38 MAPK and IL-12, IL-6, TNF-α and IL-23 secretion [32]. Thus SOCS3 induction by TLR-2 may be important for the low level of cytokine secretion induced by Lb. rhamnosus JB-1. Interestingly, not all lactobacilli strains can activate TLR-2, suggesting that strain-specific immunoregulatory effects may be partially mediated via TLR-2 activation [33].

DC-SIGN is a type II C-type lectin with a single carbohydrate recognition domain. DC-SIGN has been demonstrated to recognize a wide variety of pathogens and commensals including viruses such as HIV-1 and Ebola and bacteria such as Mycobacterium tuberculosis, Lactobacillus casei and Bifidobacterium infantis [34–36]. DC-SIGN recognizes mannose-capped lipoarabinomannan (ManLam) on Mycobacteria and activation of dendritic cells with ManLam leads to the generation of Foxp3+ Tregs involving a PGE2 dependent process [37]. DC-SIGN was previously shown to be important for lactobacillus primed MDDCs driven T regulatory cell development [38]. DC-SIGN and TLR-2 are required for IL-10 secretion and Foxp3 induction by another immunoregulatory microbe, Bifidobacterium infantis 35624 [35]. However, MDDCs process this Bifidobacterium strain very rapidly (less than 24 hours) suggesting that additional TLR-2/DC-SIGN independent Lb. rhamnosus JB-1-associated factors are responsible for the delayed intracellular processing and peri-nuclear clustering of this strain on human MDDCs.

A wide variety of Lactobacilli strains have been isolated from the human gastrointestinal tract and the majority have been shown to be commensal inhabitants of mammalian large intestine. However, certain strains have now clearly been demonstrated to exert additional beneficial effects on host immunoregulatory processes, such as that already described for Lb. rhamnosus JB-1. This microbe has shown protective effects in a range of murine models and we now describe certain potential cellular mechanisms underpinning this regulatory response. Manipulation of regulatory DC and T regulatory cell numbers or functions is an exciting therapeutic target in a wide range of inflammatory diseases [39, 40]. A clearer understanding of the mechanisms employed in vivo for the induction of oral tolerance by the microbiota will likely result in rational strategies to manipulate both regulatory and effector T cells, thereby influencing gastrointestinal disorders such as food allergy, eosinophilic esophagitis, irritable bowel syndrome and inflammatory bowel diseases.

Materials and Methods

Dendritic cell isolation and culture conditions

Monocytes and T cells were obtained from healthy volunteers. Human peripheral blood monocytes were isolated using CD14 positive isolation with the MACS system (Miltenyi Biotec, 130-050-201). Cells were cultured in cRPMI media (Life Technologies, 21875-091) with interleukin 4 1000U/ml (Novartis) and granulocyte macrophage colony stimulating factor (PeproTech, 300-03) 1000U/ml for 5–6 days in order to differentiate them into monocyte-derived dendritic cells (MDDCs). Human peripheral blood CD4 T cells were isolated using negative selection with the MACS system. Purified cells were cultured in AIM-V media (Life Technologies, 12055091). MDDCs were cultured in cRPMI and stimulated for 24 hours with different doses of Lactobacillus rhamnosus JB-1, Lactobacillus murinus (both gifts from the Alimentary Health culture collection, Cork, Ireland) or 0.5μg/ml LPS (Sigma- Aldrich). Cells were pre-incubated with the blocking monoclonal antibodies: anti-TLR2 antibody 4μg/ml (gift from C. Kirschning, Munich), anti-DC-SIGN 2μg/ml (AZDN1) (Beckman Coulter, A07406) or IgG2B control antibody, clone 20116 (R&D Systems Europe, MAB004) for 30 minutes. Cytokine secretion was examined by Bio-Plex multiplex suspension array (Bio-Rad Laboratories). The costimulatory molecules CD80 and CD86 expression on MDDCs were measured with anti-CD80 FITC and anti- CD86 PE (Beckman Coulter) by flow cytometry. MDDCs were incubated with 5x106 bacteria for 4, 8, 12, 16, 20 or 24 hours and mRNA was isolated by use of RNeasy Mini kit (Qiagen, Venlo, Netherlands). Reverse transcription was performed with Fermentas reagents, including hexamer primers (St. Leon-Rot, Germany). Real time PCR was performed with iTaq SYBR Green Supermix with ROX (Bio-Rad Laboratories, Hercules, USA) and primers: EF1a Fw: CTGAACCATCCAGGCCAAAT, EF1a Rv: GCCGTGTGGCAATCCAAT; SOCS3 Fw: TGTTTACAATCTGCCTCAATCACTCT, SOCS3 Rv: TCAAGCATCTCCTAATAGCCTCAA, synthesized by Microsynth (Balgach, Switzerland).

Phagocytosis assay

MDDCs were plated at a density of 2x106 per well in a 6-well plate. They were incubated alone or with Lactobacillus rhamnosus JB-1 or Lactobacillus murinus at 37°C, 5% CO2 for 4 hours to 24 hours. Bacteria were added at a 1:1 ratio with MDDCs. After the incubation period, MDDCs were washed with PBS, harvested and incubation with pHrodo Green E. coli BioParticles Conjugate for Phagocytosis (Molecular Probes) was performed. Flow cytometry was performed using Galios flow cytometer (Beckman Coulter). Kaluza software (Beckman Coulter) was used for the analysis of pHrodo Green E. coli BioParticles Conjugate positive cells.

Internalization assay

MDDCs were incubated alone or with Lactobacillus rhamnosus JB-1 at 37°C, 5% CO2 for 4 hours to 96 hours. Bacteria were added at a 10:1 ratio with MDDCs. After the incubation period, gentamicin (100μg/ml) was added to kill extracellular bacteria. After 2 hours, the supernatant was removed, the cells were washed with PBS and 1% Triton X-100 was used to lyse dendritic cells and allow the release of internalized bacteria. Plating of serial dilutions on MRS agar (Merck, VWR International, Dietikon, Switzerland) followed by conventional plate counting was performed.

MDDC-T cell co-cultures

MDDCs were stimulated for 4 hours with Lactobacillus rhamnosus JB-1 or Lactobacillus murinus and co-cultured with T cells from autologous donors at a ratio of 1:20 in AIM-V media. After 5 days cells were stimulated with CDMix: anti-human CD28 (generated in house), anti-human CD3 (Orthoclone OKT3, Janssen-Cilag) and anti-human CD2 (CLB-T11.2/1 and CLB-T11/1, Sanquin, M1652, M1651). Two days later cells were removed from culture and stained for CD4, CD25, Foxp3, T-bet and Ror-γt expression using flow cytometry (eBioscience, San Diego).

Bacteria labeling and visualization

Bacteria were stained with carboxyfluorescein diacetate, carboxyfluorescein succinimidyl ester (CFSE) (Life technologies, C1157), while MDDCs were stained with anti-human CD11c PE-Cy5, clone B-ly6 (BD Pharmingen). MDDCs were incubated with CFSE-labeled bacteria for 4 hours in HBSS with or without calcium and magnesium. Binding was analyzed flow cytometry. Moreover, bacteria binding in cRPMI was visualized after 24 and 72 hours by use of multispectral imaging flow cytometer Image Stream X (Amnis Corporation) and images were analyzed with IDEAS software (Amnis Corporation). MDDCs were plated on round cover slips and incubated with bacteria for 4, 24, 48 or 96 hours with or without blocking monoclonal antibodies. Cells were additionally stained with DAPI in ProLong Gold antifade reagent (Life Technologies, P36935). Slides were analyzed by confocal microscopy.

HEK-293 cells

HEK-Blue hTLR2 cells and HEK-Blue Null1 cells (Invivogen) were pre-incubated with anti-TLR2 antibody for 30 minutes and were stimulated with 1x105 bacteria for 24 hours. Both cell lines express NF-κB-inducible secreted embryonic alkaline phosphatase (SEAP). NF-κB induction was measured indirectly by quantifying the enzymatic reaction with Quanti blue reagent (Invivogen, rep-qb1) and spectrophotometry.

Statistical analysis

Unpaired student t-tests were used to compare bacterial-stimulated MDDC cytokine secretion levels. Wilcoxon matched-pairs test was used to evaluate the effect of blocking antibodies on activated dendritic cells. All data analysis was performed using GraphPad Prism software.

Supporting Information

S1 Fig. Lb. rhamnosus JB-1-stimulated MDDCs upregulated SOCS gene expression and p38 MAPK responses were significantly less than for LPS stimulated cells.

(TIF)

Click here for additional data file. (127.1KB, tif)

Data Availability

All relevant data are within the paper and on Figshare via http://dx.doi.org/10.6084/m9.figshare.1295392

Funding Statement

The authors are supported by Swiss National Foundation grants (project numbers 310030-127356 and 310030_144219), Allergiestiftung Ulrich Müller-Gierok, European Union research grants and EU Marie Curie grants. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

References

  • 1. Lee YK, Mazmanian SK. Has the microbiota played a critical role in the evolution of the adaptive immune system? Science 2010;330: 1768–1773. 10.1126/science.1195568 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2. Shanahan F. Gut microbes: from bugs to drugs. Am J Gastroenterol. 2010;105: 275–279. 10.1038/ajg.2009.729 [DOI] [PubMed] [Google Scholar]
  • 3. Sommer F, Bäckhed F. The gut microbiota—masters of host development and physiology. Nat Rev Microbiol. 2013;11: 227–238. 10.1038/nrmicro2974 [DOI] [PubMed] [Google Scholar]
  • 4. Kamada N, Chen GY, Inohara N, Núñez G. Control of pathogens and pathobionts by the gut microbiota. Nat Immunol. 2013;14: 685–690. 10.1038/ni.2608 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5. Pridmore RD, Berger B, Desiere F, Vilanova D, Barretto C, Pittet AC, et al. The genome sequence of the probiotic intestinal bacterium Lactobacillus johnsonii NCC 533. Proc Natl Acad Sci U S A. 2004;101: 2512–2517. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6. Peterson LW, Artis D. Intestinal epithelial cells: regulators of barrier function and immune homeostasis. Nat Rev Immunol. 2014;14: 141–153. 10.1038/nri3608 [DOI] [PubMed] [Google Scholar]
  • 7. Pluznick J. A novel SCFA receptor, the microbiota, and blood pressure regulation. Gut Microbes 2013;5: 202–207. 10.4161/gmic.27492 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8. Frei R, Lauener RP, Crameri R, O'Mahony L. Microbiota and dietary interactions: an update to the hygiene hypothesis? Allergy 2012;67: 451–461. 10.1111/j.1398-9995.2011.02783.x [DOI] [PubMed] [Google Scholar]
  • 9. Brestoff JR, Artis D. Commensal bacteria at the interface of host metabolism and the immune system. Nat Immunol. 2013;14: 676–684. 10.1038/ni.2640 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10. Sakaguchi S, Miyara M, Costantino CM, Hafler DA. FOXP3+ regulatory T cells in the human immune system. Nat Rev Immunol. 2010;10: 490–500. 10.1038/nri2785 [DOI] [PubMed] [Google Scholar]
  • 11. Akdis M, Verhagen J, Taylor A, Karamloo F, Karagiannidis C, Crameri R, et al. Immune responses in healthy and allergic individuals are characterized by a fine balance between allergen-specific T regulatory 1 and T helper 2 cells. J Exp Med. 2004;199: 1567–1575. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12. Atarashi K, Tanoue T, Shima T, Imaoka A, Kuwahara T, Momose Y, et al. Induction of colonic regulatory T cells by indigenous Clostridium species. Science. 2011;331: 337–341. 10.1126/science.1198469 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13. van Baarlen P, Wells JM, Kleerebezem M. Regulation of intestinal homeostasis and immunity with probiotic lactobacilli. Trends Immunol. 2013;34: 208–215. 10.1016/j.it.2013.01.005 [DOI] [PubMed] [Google Scholar]
  • 14. Inman MD, Bienenstock J, Forsythe P. Lactobacillus reuteri-induced regulatory T cells protect against an allergic airway response in mice. Am J Respir Crit Care Med. 2009;179: 186–193. 10.1164/rccm.200806-951OC [DOI] [PubMed] [Google Scholar]
  • 15. Karimi K, Kandiah N, Chau J, Bienenstock J, Forsythe P. A Lactobacillus rhamnosus strain induces a heme oxygenase dependent increase in Foxp3+ regulatory T cells. PLoS One 2012;7: e47556 10.1371/journal.pone.0047556 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16. Van der Kleij H, O’Mahony C, Shanahan F, O’Mahony L, Bienenstock J. Protective effects of Lactobacillus rhamnosus and Bifidobacterium infantis in murine models for colitis do not involve the vagus nerve. Am J Physiol Regul Integr Comp Physiol. 2008;295: R1131–1137. 10.1152/ajpregu.90434.2008 [DOI] [PubMed] [Google Scholar]
  • 17. Bravo JA, Forsythe P, Chew MV, Escaravage E, Savignac HM, Dinan TG, et al. Ingestion of Lactobacillus strain regulates emotional behavior and central GABA receptor expression in a mouse via the vagus nerve. Proc. Natl. Acad. Sci. USA 2011;108: 16050–16055. 10.1073/pnas.1102999108 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18. Lyons A, O'Mahony D, O'Brien F, MacSharry J, Sheil B, Ceddia M, et al. Bacterial strain-specific induction of Foxp3+ T regulatory cells is protective in murine allergy models. Clin Exp Allergy 2010;40: 811–819. 10.1111/j.1365-2222.2009.03437.x [DOI] [PubMed] [Google Scholar]
  • 19. Macho Fernandez E, Valenti V, Rockel C, Hermann C, Pot B, Boneca IG, et al. Anti-inflammatory capacity of selected lactobacilli in experimental colitis is driven by NOD2- mediated recognition of a specific peptidoglycan-derived muropeptide. Gut 2011;60: 1050–1059. 10.1136/gut.2010.232918 [DOI] [PubMed] [Google Scholar]
  • 20. Grangette C, Nutten S, Palumbo E, Morath S, Hermann C, Dewulf J, et al. Enhanced antiinflammatory capacity of a Lactobacillus plantarum mutant synthesizing modified teichoic acids. Proc Natl Acad Sci U S A 2005;102: 10321–10326. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21. Khan MW, Zadeh M, Bere P, Gounaris E, Owen J, Klaenhammer T, et al. Modulating intestinal immune responses by lipoteichoic acid-deficient Lactobacillus acidophilus. Immunotherapy 2012;4: 151–161. 10.2217/imt.11.163 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22. Yan F, Polk DB. Probiotic bacterium prevents cytokine induced apoptosis in intestinal epithelial cells. J Biol Chem. 2002;277: 50959–50965. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23. Yan F, Cao H, Cover TL, Whitehead R, Washington MK, Polk DB. Soluble proteins produced by probiotic bacteria regulate intestinal epithelial cell survival and growth. Gastroenterology 2007;132: 562–575. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24. Yan F, Cao H, Cover TL, Washington MK, Shi Y, Liu L, et al. Colon-specific delivery of a probiotic-derived soluble protein ameliorates intestinal inflammation in mice through an EGFR-dependent mechanism. J Clin Invest. 2011;121: 2242–2253. 10.1172/JCI44031 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25. Meijerink M, van Hemert S, Taverne N, Wels M, de Vos P, Bron PA, et al. Identification of genetic loci in Lactobacillus plantarum that modulate the immune response of dendritic cells using comparative genome hybridization. PLoS One 2010;5: e10632 10.1371/journal.pone.0010632 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26. Konstantinov SR, Smidt H, de Vos WM, Bruijns SC, Singh SK, Valence F, et al. S layer protein A of Lactobacillus acidophilus NCFM regulates immature dendritic cell and T cell functions. Proc Natl Acad Sci U S A. 2008;105: 19474–19479. 10.1073/pnas.0810305105 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27. Frei R, Ferstl R, Konieczna P, Ziegler M, Simon T, Rugeles TM, et al. Histamine receptor 2 modifies dendritic cell responses to microbial ligands. J Allergy Clin Immunol. 2013;132: 194–204. 10.1016/j.jaci.2013.01.013 [DOI] [PubMed] [Google Scholar]
  • 28. Ferstl R, Frei R, Schiavi E, Konieczna P, Barcik W, Ziegler M, et al. Histamine 2 receptor is a key influence in immune responses to intestinal histamine-secreting microbes. J Allergy Clin Immunol. 2014;134: 744–746. 10.1016/j.jaci.2014.04.034 [DOI] [PubMed] [Google Scholar]
  • 29. Schiavi E, Smolinska S, O'Mahony L. Intestinal dendritic cells. Curr Opin Gastroenterol. 2015;31: 98–103. 10.1097/MOG.0000000000000155 [DOI] [PubMed] [Google Scholar]
  • 30. Round JL, Lee SM, Li J, Tran G, Jabri B, Chatila TA, et al. The Toll-like receptor 2 pathway establishes colonization by a commensal of the human microbiota. Science. 2011;332: 974–977. 10.1126/science.1206095 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31. Round JL, Mazmanian SK. Inducible Foxp3+ regulatory T-cell development by a commensal bacterium of the intestinal microbiota. Proc Natl Acad Sci U S A. 2010;107: 12204–12209. 10.1073/pnas.0909122107 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32. Manicassamy S, Ravindran R, Deng J, Oluoch H, Denning TL, Kasturi SP, et al. Toll-like receptor 2-dependent induction of vitamin A-metabolizing enzymes in dendritic cells promotes T regulatory responses and inhibits autoimmunity. Nat Med. 2009;15: 401–409. 10.1038/nm.1925 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33. van Bergenhenegouwen J, Kraneveld AD, Rutten L, Kettelarij N, Garssen J, Vos AP. Extracellular vesicles modulate host-microbe responses by altering TLR2 activity and phagocytosis. PLoS One 2014;9: e89121 10.1371/journal.pone.0089121 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34. Koppel EA, van Gisbergen K, Geijtenbeek TBH, van Kooyk Y. Distinct functions of DC-SIGN and its homologues L-SIGN (DC-SIGNR) and mSIGNR1 in pathogen recognition and immune regulation. Cell. Microbiol. 2005;7: 157–165. [DOI] [PubMed] [Google Scholar]
  • 35. Konieczna P, Groeger D, Ziegler M, Frei R, Ferstl R, Shanahan F, et al. Bifidobacterium infantis 35624 administration induces Foxp3 T regulatory cells in human peripheral blood: potential role for myeloid and plasmacytoid dendritic cells. Gut. 2012; 61: 354–366. 10.1136/gutjnl-2011-300936 [DOI] [PubMed] [Google Scholar]
  • 36. Konieczna P, Akdis CA, Quigley EM, Shanahan F, O'Mahony L. Portrait of an immunoregulatory Bifidobacterium. Gut Microbes 2012;3: 261–266. 10.4161/gmic.20358 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37. Garg A, Barnes PF, Roy S, Quiroga MF, Wu S, García VE, et al. Mannose-capped lipoarabinomannan- and prostaglandin E2-dependent expansion of regulatory T cells in human Mycobacterium tuberculosis infection. Eur J Immunol. 2008;38: 459–469. 10.1002/eji.200737268 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38. Smits HH, Engering A, van der Kleij D, de Jong EC, Schipper K, van Capel TM, et al. Selective probiotic bacteria induce IL-10-producing regulatory T cells in vitro by modulating dendritic cell function through dendritic cell-specific intercellular adhesion molecule 3-grabbing nonintegrin. J Allergy Clin Immunol. 2005;115: 1260–1267. [DOI] [PubMed] [Google Scholar]
  • 39. Akdis M, Akdis CA. Therapeutic manipulation of immune tolerance in allergic disease. Nat Rev Drug Discov. 2009;8: 645–660. 10.1038/nrd2653 [DOI] [PubMed] [Google Scholar]
  • 40. O'Mahony L, Akdis M, Crameri R, Akdis CA. Novel immunotherapeutic approaches for allergy and asthma. Autoimmunity 2010;43: 493–503. 10.3109/08916931003674725 [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

S1 Fig. Lb. rhamnosus JB-1-stimulated MDDCs upregulated SOCS gene expression and p38 MAPK responses were significantly less than for LPS stimulated cells.

(TIF)

Click here for additional data file. (127.1KB, tif)

Data Availability Statement

All relevant data are within the paper and on Figshare via http://dx.doi.org/10.6084/m9.figshare.1295392

Articles from PLoS ONE are provided here courtesy of PLOS

RESOURCES